Fedor Nikulenkov

971 total citations
12 papers, 768 citations indexed

About

Fedor Nikulenkov is a scholar working on Molecular Biology, Oncology and Biotechnology. According to data from OpenAlex, Fedor Nikulenkov has authored 12 papers receiving a total of 768 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Oncology and 2 papers in Biotechnology. Recurrent topics in Fedor Nikulenkov's work include Cancer-related Molecular Pathways (6 papers), RNA modifications and cancer (4 papers) and DNA Repair Mechanisms (4 papers). Fedor Nikulenkov is often cited by papers focused on Cancer-related Molecular Pathways (6 papers), RNA modifications and cancer (4 papers) and DNA Repair Mechanisms (4 papers). Fedor Nikulenkov collaborates with scholars based in Sweden, United States and Czechia. Fedor Nikulenkov's co-authors include Galina Selivanova, Alexander Kel, Vera Grinkevich, Joanna Zawacka‐Pankau, Yao Shi, Wenjie Bao, Martin Enge, Haitao Li, Elisabeth Hedström and Clemens Spinnler and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Cancer Cell.

In The Last Decade

Fedor Nikulenkov

12 papers receiving 761 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Fedor Nikulenkov Sweden 10 596 369 180 64 51 12 768
Sylvain Peuget Sweden 11 400 0.7× 269 0.7× 155 0.9× 73 1.1× 44 0.9× 17 601
Angelo Lupo Italy 16 673 1.1× 199 0.5× 126 0.7× 49 0.8× 33 0.6× 32 880
Min-Sik Lee South Korea 10 491 0.8× 179 0.5× 166 0.9× 53 0.8× 28 0.5× 14 629
Gastón Soria Argentina 15 968 1.6× 316 0.9× 163 0.9× 35 0.5× 26 0.5× 27 1.1k
Susumu Rokudai Japan 16 742 1.2× 386 1.0× 177 1.0× 62 1.0× 73 1.4× 29 1.0k
Hsu-Ping Kuo United States 12 892 1.5× 274 0.7× 187 1.0× 67 1.0× 45 0.9× 12 1.1k
Perry Stambolsky Israel 11 700 1.2× 588 1.6× 272 1.5× 54 0.8× 55 1.1× 14 1.0k
Niels van den Broek United Kingdom 6 597 1.0× 171 0.5× 166 0.9× 57 0.9× 30 0.6× 7 696
Kyung Hee Koo South Korea 9 487 0.8× 194 0.5× 245 1.4× 39 0.6× 84 1.6× 11 760
Danupon Nantajit United States 11 561 0.9× 345 0.9× 232 1.3× 50 0.8× 118 2.3× 20 928

Countries citing papers authored by Fedor Nikulenkov

Since Specialization
Citations

This map shows the geographic impact of Fedor Nikulenkov's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Fedor Nikulenkov with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fedor Nikulenkov more than expected).

Fields of papers citing papers by Fedor Nikulenkov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fedor Nikulenkov. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Fedor Nikulenkov. The network helps show where Fedor Nikulenkov may publish in the future.

Co-authorship network of co-authors of Fedor Nikulenkov

This figure shows the co-authorship network connecting the top 25 collaborators of Fedor Nikulenkov. A scholar is included among the top collaborators of Fedor Nikulenkov based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Fedor Nikulenkov. Fedor Nikulenkov is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

12 of 12 papers shown
1.
Son, Mi‐Young, Ondrej Beláň, Mário Špı́rek, et al.. (2024). RAD51 separation of function mutation disables replication fork maintenance but preserves DSB repair. iScience. 27(4). 109524–109524. 2 indexed citations
2.
Marini, Victoria, et al.. (2023). MUS81 cleaves TOP1-derived lesions and other DNA–protein cross-links. BMC Biology. 21(1). 110–110. 7 indexed citations
3.
Bereshchenko, Oxana, Oriana Lo Re, Fedor Nikulenkov, et al.. (2019). Deficiency and haploinsufficiency of histone macroH2A1.1 in mice recapitulate hematopoietic defects of human myelodysplastic syndrome. Clinical Epigenetics. 11(1). 121–121. 22 indexed citations
4.
Hengel, Sarah R, Mário Špı́rek, Fedor Nikulenkov, et al.. (2019). DSS1 interacts with and stimulates RAD52 to promote the repair of DSBs. Nucleic Acids Research. 48(2). 694–708. 25 indexed citations
5.
Shi, Yao, Fedor Nikulenkov, Joanna Zawacka‐Pankau, et al.. (2014). ROS-dependent activation of JNK converts p53 into an efficient inhibitor of oncogenes leading to robust apoptosis. Cell Death and Differentiation. 21(4). 612–623. 187 indexed citations
6.
Sarangi, Prabha, Peter Kolesár, Danuša Vlasáková, et al.. (2013). Lif1 SUMOylation and its role in non-homologous end-joining. Nucleic Acids Research. 41(10). 5341–5353. 13 indexed citations
7.
Nikulenkov, Fedor, Clemens Spinnler, Claudia Tonelli, et al.. (2012). Insights into p53 transcriptional function via genome-wide chromatin occupancy and gene expression analysis. Cell Death and Differentiation. 19(12). 1992–2002. 157 indexed citations
8.
Zawacka‐Pankau, Joanna, Vera Grinkevich, Sabine Hünten, et al.. (2011). Inhibition of Glycolytic Enzymes Mediated by Pharmacologically Activated p53. Journal of Biological Chemistry. 286(48). 41600–41615. 103 indexed citations
9.
Spinnler, Clemens, Elisabeth Hedström, Haitao Li, et al.. (2011). Abrogation of Wip1 expression by RITA-activated p53 potentiates apoptosis induction via activation of ATM and inhibition of HdmX. Cell Death and Differentiation. 18(11). 1736–1745. 33 indexed citations
10.
Grinkevich, Vera, et al.. (2010). Rescue of the apoptotic-inducing function of mutant p53 by small molecule RITA. Cell Cycle. 9(9). 1847–1855. 68 indexed citations
11.
Grinkevich, Vera, Fedor Nikulenkov, Yao Shi, et al.. (2009). Ablation of Key Oncogenic Pathways by RITA-Reactivated p53 Is Required for Efficient Apoptosis. Cancer Cell. 15(5). 441–453. 93 indexed citations
12.
Поспелова, Т. В., et al.. (2006). G1/S Arrest Induced by Histone Deacetylase Inhibitor Sodium Butyrate in E1A + Ras-transformed Cells Is Mediated through Down-regulation of E2F Activity and Stabilization of β-Catenin. Journal of Biological Chemistry. 281(30). 21040–21051. 58 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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